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Experience Required for Your SuccessRequirements:BS in chemical or biochemical engineering, or related degree supplemented with relevant experience (MS in engineering preferred)Experience in pharmaceutical/biopharmaceutical industry or related industry/cGMP environmentDemonstrated experience with manufacturing processes and equipment such as CIP systems, filtration skids, chromatography and lyophilization equipment, etc.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Quality Assurance Manager will ensure compliance with current Good Manufacturing Practices (cGMP) as they pertain to the local regulation and exporting countries regulation as applicable (such as FDA, MHRA, EMA, Health Canada.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Document all testing activities in accordance with cGMP.Performs duties according to LSS Global direction and in compliance with cGMP and GLP regulations and SGS Integrity programs. Job DescriptionThe Chemist I, Extractable & Leachable will perform material extractions, standard solution, and sample preparations to support GC-MS/FID and/or LC-MS/PDA and/or ICP-MS/OES analysis on extractable and leachable (E&L) testing of pharmaceutical containers and medical devices.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Compiled standard operating procedures based on cGMP and HACCP requirements, and established the laboratory in functioning capacity. Host FDA inspections, and compile a set of standard operating procedures based on cGMP guidelines, and validated operating systems.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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5-7 years of cGMP environment, aseptic processing, mammalian cell culture, cell processing, cryopreservation experience. Deep understanding of cGMP and cGLP. Bachelor's degree (ie Biology, Biotechnology, Bioengineering, Chemical Engineering.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Personal responsibility for following safety rules, SOP's and cGMP guidelines. Our broad product portfolio includes renowned brands like Garden of Life®, Nature's Bounty®, Vital Proteins®, Orgain®, Nuun®, BOOST®, Carnation Breakfast Essentials®, Peptamen®, Compleat Organic Blends®, and more.
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In addition, our team also works on projects with clients to manage these Quality business processes for supply chain, manufacturing, commercial operations and R&D. This includes analyzing various cGMP and 21 CFR Part 11 regulations in the Regulatory Compliance area to determine impact on risk exposure.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Knowledge of GCP and global cGMP regulations, (knowledge of EU GMP QP regulations is preferred), a plus. Knowledge of the operation and technical theory for the following analytical chemistry instruments: KF, FTIR, HPLC, GC, LC/MS, PSD, XRD, and DSC.
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Assist and support Associate Director in managing Contract Development and Research Organizations (CDMO) in the areas of Analytical Chemistry Method Development and Clinical Trial Material (CTM) manufacturing.
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Skills : Cell processing, clinical cell therapy, gene therapy, biologics. Meet client process demands through planning, scheduling, manufacture and delivery of clinical cell therapy products according to established procedures, regulations and contract.
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Our extensive product portfolio includes renowned brands like Garden of Life®, Nature's Bounty®, Vital Proteins®, Orgain®, Nuun®, BOOST®, Carnation Breakfast Essentials®, Peptamen®, Compleat Organic Blends®, and more.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Familiarity of industry standards such as cGMP, IQ/OQ, ASME, UL/CE, BPE, FDA). 6 to 7+ years of experience in industrial capital equipment sales. Support, train, coach, and motivate CPS staff & DCI sales team personnel.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Manufacturing Operator/Technician II is responsible for all functions relating to the processing of drug products; consistent with established Current Good Manufacturing Practices (cGMP), customer requirements and in conjunction with all Standard Operating Procedures (SOP.
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In support of our main functions, additional responsibilities include maintain compliance with all applicable Regulatory requirements relative to FDA, cGMP Regulations, Company's SOPs and Safety Regulations, accurate documentation on batch production records and logs, and cleaning and maintain production areas.
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Partner with DCI to create sales strategies and successful proposals for current and prospective customers within the assigned territory. Support the lead generation, quotation, negotiation, and closing of sales for major customers, engineering firms and/or other equipment manufacturers/suppliers.
Full-timeExpandApply NowActive JobUpdated 1 month ago
cgmp job in Saddle Brook, NJ
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